Clinical Research Coordinator (Data Entry)

SHIFT:Day (United States of America) Seeking Breakthrough Makers Children's Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation. CHOP does not discriminate on the basis of race, color, sex, national origin, religion, or any other legally protected categories in any employment, training, or vendor decisions or programs. The Children's Hospital of Philadelphia, Division of Hematology, is hiring a full-time clinical research coordinator. The research coordinator will work with clinical studies involving thalassemia and other red blood cell disorders, as well as coordinate sample collection and processing for the Division of Hematology Biorepository. Specific research projects will be discussed at the time of interview. It may also include travel to hematology conferences, authorship and publishing opportunities. There is a component of basic wet lab work to process samples and run simple assays. Opportunities are available to attend weekly Hematology Divisional Clinical Conference and weekly Department of Pediatrics Grand Rounds, which provide unique insight into a large tertiary pediatric hospital. Research staff are required to attend disease program weekly clinical meetings. Support the safety of clinical research patients/research participants Coordinate protocol related research procedures, study visits, and follow-up care Screen, recruit and enroll patients/research participants Maintain study source documents Understand good clinical practice (GCP) and regulatory compliance Comply with Institutional policies, standard operating procedures (SOPs) and guidelines Must comply with federal, state, and sponsor policies Prepare, manage, submit, and maintain essential regulatory documents (e.g. and remain aware of the regulatory status for projects within scope of role Register study on ClinicalTrial.Complete case report forms (paper & electronic data capture) and address queries Facilitate pre-study, site qualification, study initiation, and monitoring visit as appropriate Coordinate research/project team meetings Collect, process and ship laboratory specimens Retain records/archive documents after study close out Manage study finances including sponsor invoicing & resolving study subject billing issues Develop advertisement materials Act as liaison for research subject, investigator, IRB, sponsor, and healthcare professionals Organize and/or run study-related meetings locally or across teams (for multi-site projects) Support study team communications and outreach Provide training to junior staff on conduct of research studies Document investigational product (drug/device) accountability Develop informed consent document and/or draft or edit IRB protocols or related documents such as study administration manuals Maintain Clinical Trial.Bachelor's Degree Required Master's Degree in a related field Preferred At least two (2) years of clinical/research coordination experience Required At least three (3) years of clinical/research coordination experience Preferred To carry out its mission, CHOP is committed to supporting the health of our patients, families, workforce, and global community. EEO / VEVRAA Federal Contractor | Tobacco Statement 58,300.00 - $72,900.00 Annually Salary ranges are shown for full-time jobs. If you're working part-time, your pay will be adjusted accordingly.